Executive, Quality Control

4 days ago

Bandar Baru Enstek, Malaysia Novugen Oncology Sdn Bhd Full time

**About us**

Novugen is a wholly owned subsidiary of SciTech International, a UAE-based group with over 30 years of experience in the healthcare industry. We specialize in venturing into strategic healthcare businesses and developing world-class healthcare facilities across the globe. With operations in multiple countries across continents, our global presence and expertise empower us to meet the complex challenges of delivering hard-to-source, technology-intensive pharmaceutical products to market.

Our manufacturing facilities in Bandar Enstek, Negeri Sembilan, are the first USFDA-approved pharmaceutical manufacturing facilities in Malaysia and Southeast Asia. We are also the first pharmaceutical company in the region to be vertically integrated from R&D to manufacturing, giving us greater control over the supply chain and reflecting our commitment to meeting a wide range of stringent regulatory standards.

At Novugen, we are united by a shared vision, with a team of talented individuals from diverse backgrounds and nationalities working together towards one common goal. We are driven by a passion for science and innovation, striving to accelerate the launch of pharmaceuticals that lack robust generic alternatives due to their complexity. Our continued investment in R&D and dedication to excellence aim to provide early access to affordable, high-quality medicines, impact lives across the world.

Together, we are shaping the future of healthcare and changing lives everywhere.

**About the role**

The Executive, Quality Control will oversee Quality control activities such as calibration, verification and standardization and comply with GMP, GLP procedures and other regulatory requirements within In-Proces & Finished Goods section.

Key Responsibilities:
- Assist QC Manager in the management and administration of the QC Laboratory.
- Ensure the cleanliness of working area, verification of calibration status, maintenance of workspaces and preventive maintenance status of the instruments.
- Responsible to management of chemicals, HPLC and GC Column, reference standard and working standard as per the SOP.
- Responsible to perform the daily verification, calibration, and maintenance of instruments/equipment’s activities as per the schedule.
- Responsible to perform the analysis for working standard, raw materials, in-process, finished product and stability samples as per predefined procedures.
- Responsible to review and verified logbook in QC Lab.
- Responsible to calibration, and maintenance of stability chamber
- Responsible to prepare of the new and revision of SOPs for improvement of GLP compliance and revisions.
- Responsible to ensure good documentation practices in all QC documents and ensure real-time documentation completion.
- Responsible to initiate purchase requisition through SAP system.

Perform other related duties as assigned from time to time based on company needs

**About you**
- Minimum 1 year of working experience preferably in Pharmaceutical Manufacturing/ Medical Device industry.
- Hands on exposure in HPLC, GC, FTIR, UV-Vis, Stability and IP/FP will be an added advantage.
- Fresh Graduate with relevant internship experience are welcome to apply.
- Proficient in Microsoft Office Suite.
- Must be willing to work at Bandar Baru Enstek, Negeri Sembilan.

Pay: RM2,300.00 - RM3,500.00 per month

Schedule:

- Monday to Friday

Work Location: In person

Expected Start Date: 08/03/2025

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